Taiwan FDA registration 37d225a5f51611008ae5578fa6df5bd2
"Neop" new jama ray detection system (unsterilized)
TW: “尼歐普”新珈碼射線偵測系統(未滅菌)
Taiwan·Risk Class 1·NEOPROBE CORPORATION·Registered Jun 25, 2008 – Jun 25, 2013CancelledRegistration details
- Analysis ID
- 37d225a5f51611008ae5578fa6df5bd2
- Customs Code
- DHA04400683305
Company information
- Manufacturer
- NEOPROBE CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Defeng Technology Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of nuclear medical ingestion probe (P.1320) under the management measures for medical equipment.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1320 核醫攝取探頭
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jun 25, 2008
- Expiry Date
- Jun 25, 2013
- Cancellation Date
- Jun 17, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Neop" new jama ray detection system (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 37d225a5f51611008ae5578fa6df5bd2 and manufactured by NEOPROBE CORPORATION. The authorized representative in Taiwan is Defeng Technology Co., Ltd.
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